药品注册申请号:009866
申请类型:NDA (新药申请)
申请人:PHARMACIA AND UPJOHN
申请人全名:PHARMACIA AND UPJOHN CO
产品信息
产品号商品名活性成分剂型/给药途径规格/剂量参比药物(RLD)生物等效参考标准(RS)治疗等效代码该申请号批准日期该产品号批准日期市场状态
001 SOLU-CORTEF HYDROCORTISONE SODIUM SUCCINATE INJECTABLE;INJECTION EQ 100MG BASE/VIAL Yes Yes AP 1955/04/27 Approved Prior to Jan 1, 1982 Prescription
002 SOLU-CORTEF HYDROCORTISONE SODIUM SUCCINATE INJECTABLE;INJECTION EQ 250MG BASE/VIAL Yes Yes None Approved Prior to Jan 1, 1982 Prescription
003 SOLU-CORTEF HYDROCORTISONE SODIUM SUCCINATE INJECTABLE;INJECTION EQ 500MG BASE/VIAL Yes Yes None Approved Prior to Jan 1, 1982 Prescription
004 SOLU-CORTEF HYDROCORTISONE SODIUM SUCCINATE INJECTABLE;INJECTION EQ 1GM BASE/VIAL Yes Yes None Approved Prior to Jan 1, 1982 Prescription
批准日期,申请提交历史,通知信,药品说明书,审评文件等信息
提交状态日期提交号审批结论申请内容分类审评优先级;罕用药状态通知信、审评文件、说明书、包装标签备注
2024/07/10 SUPPL-120(补充) Approval Labeling STANDARD
2024/06/05 SUPPL-121(补充) Approval Labeling STANDARD
2023/12/20 SUPPL-119(补充) Approval Labeling STANDARD
2021/05/27 SUPPL-115(补充) Approval Labeling STANDARD
2019/11/21 SUPPL-113(补充) Approval Labeling STANDARD
2016/09/08 SUPPL-105(补充) Approval Labeling STANDARD
2016/09/08 SUPPL-98(补充) Approval Labeling STANDARD
2016/02/25 SUPPL-108(补充) Approval Manufacturing (CMC) STANDARD
2015/09/23 SUPPL-90(补充) Approval Manufacturing (CMC) STANDARD
2014/09/06 SUPPL-92(补充) Approval Manufacturing (CMC) STANDARD
2014/07/22 SUPPL-101(补充) Approval Manufacturing (CMC) STANDARD
2014/07/03 SUPPL-104(补充) Approval Labeling STANDARD
2014/06/24 SUPPL-103(补充) Approval Manufacturing (CMC) STANDARD
2014/06/09 SUPPL-102(补充) Approval Manufacturing (CMC) STANDARD
2014/04/04 SUPPL-95(补充) Approval Manufacturing (CMC) STANDARD
2014/03/28 SUPPL-99(补充) Approval Manufacturing (CMC) STANDARD
2013/11/08 SUPPL-96(补充) Approval Manufacturing (CMC) STANDARD
2013/09/27 SUPPL-97(补充) Approval Manufacturing (CMC) STANDARD
2010/06/16 SUPPL-80(补充) Approval Manufacturing (CMC) STANDARD
2009/09/01 SUPPL-79(补充) Approval Labeling STANDARD
2009/09/01 SUPPL-77(补充) Approval Labeling STANDARD
2002/10/21 SUPPL-72(补充) Approval Manufacturing (CMC) STANDARD
2000/04/04 SUPPL-71(补充) Approval Manufacturing (CMC) STANDARD
1999/11/25 SUPPL-70(补充) Approval Manufacturing (CMC) STANDARD
1994/12/06 SUPPL-62(补充) Approval Manufacturing (CMC) STANDARD
1994/09/15 SUPPL-67(补充) Approval Manufacturing (CMC) STANDARD
1994/03/25 SUPPL-65(补充) Approval Manufacturing (CMC) STANDARD
1993/12/28 SUPPL-61(补充) Approval Labeling
1991/04/01 SUPPL-59(补充) Approval Manufacturing (CMC) STANDARD
1990/03/29 SUPPL-56(补充) Approval Manufacturing (CMC) STANDARD
1990/01/16 SUPPL-57(补充) Approval Manufacturing (CMC) STANDARD
1989/03/22 SUPPL-50(补充) Approval Labeling
1988/05/13 SUPPL-55(补充) Approval Manufacturing (CMC) STANDARD
1987/07/23 SUPPL-52(补充) Approval Manufacturing (CMC) STANDARD
1987/07/02 SUPPL-54(补充) Approval Manufacturing (CMC) STANDARD
1985/07/24 SUPPL-51(补充) Approval Labeling
1981/12/15 SUPPL-47(补充) Approval Labeling
1981/12/15 SUPPL-46(补充) Approval Manufacturing (CMC) STANDARD
1980/04/14 SUPPL-45(补充) Approval Labeling
1979/09/24 SUPPL-44(补充) Approval Manufacturing (CMC) STANDARD
1979/06/18 SUPPL-43(补充) Approval Manufacturing (CMC) STANDARD
1955/04/27 ORIG-1(原始申请) Approval Type 2 - New Active Ingredient STANDARD
与本品相关的专利信息(来自FDA橙皮书Orange Book)
关联产品号专利号专利过期日是否物质专利是否产品专利专利用途代码撤销请求提交日期专利下载备注
与本品相关的市场独占权保护信息
关联产品号独占权代码失效日期备注
与本品治疗等效的药品
活性成分:HYDROCORTISONE SODIUM SUCCINATE 剂型/给药途径:INJECTABLE;INJECTION 规格:EQ 100MG BASE/VIAL 治疗等效代码:AP
申请号产品号申请类型商品名活性成分剂型/给药途径规格市场状态RLDRSTE Code产品号批准日期申请人
009866 001 NDA SOLU-CORTEF HYDROCORTISONE SODIUM SUCCINATE INJECTABLE;INJECTION EQ 100MG BASE/VIAL Prescription Yes Yes AP Approved Prior to Jan 1, 1982 PHARMACIA AND UPJOHN
214050 001 ANDA HYDROCORTISONE SODIUM SUCCINATE HYDROCORTISONE SODIUM SUCCINATE INJECTABLE;INJECTION EQ 100MG BASE/VIAL Prescription No No AP 2024/09/05 CIPLA
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